Correlation of University of Texas Cancer Cachexia Staging (UTCCS) with clinical variables of systemic inflammation, nutritional status, and physical function in patients with cancer cachexia.

H Harshit Khosla (2University of Texas Helath Science Center at Houston Medical, houston, United States) S Syed Hasan Raza Jafri (University of Texas, Houston, TX) J Julie Haewon Rowe (The University of Texas Health Science Center at Houston (UTHealth Houston) McGovern Medical School, Houston, TX) P Putao Cen (The University of Texas Health Science Center at Houston (UTHealth Houston) McGovern Medical School, Houston, TX) J Jessica Trevino Jones (UT San Antonio, San Antonio, TX) A Anneliese Gonzalez (University of Texas Medical School at Houston, Houston, TX) N Neha Maithel (University of Texas at Houston Health Science Center, McGovern Medical School, Houston, TX) R Rabab Jafry (Aga Khan University Hospital, Karachi, Pakistan) B Betty Arceneaux (UT Health, Houston, TX) S Shahroz Aziz (The University of Texas Health Science Center at Houston, Houston, TX) M Mina Hanna (The University of Texas Health Science Center at Houston, Houston, TX) A Amirali Tahanan (The University of Texas Health Science Center at Houston, Houston, TX) Y Yi-Ping Li M Mohammad Hossein Rahbar (The University of Texas Health Science Center at Houston, Houston, TX)

Abstract

12046 Background: Cancer cachexia is a heterogenous syndrome characterized by ongoing loss of skeletal mass with or without adipose tissue, that is not entirely reversible. University of Texas Cancer Cachexia Staging (UTCCS) is a recently described novel model for staging cachexia using simple clinical parameters such as body mass index (BMI), serum albumin (alb), neutrophil to lymphocyte ratio (NLR) and resting heart rate (RHR). The validity of this model to correlate with functional status, nutrition and overall survival in patients with advanced or metastatic cancer has been assessed in current study. Methods: In a prospective study of newly diagnosed cancer patients with stage III/IV cancers, >5% body weight loss and serum albumin < 3.5g/dL biomarkers of cachexia were identified. UTCCS was developed using 4 clinical variables namely (BMI), (Alb), (NLR) and (RHR) using quartile as cut off. Based on these variable patients were categorized into stage I, stage II or stage III cancer cachexia. Blood biomarkers, dietary assessment and functional status were estimated. Kaplan-Meier survival curves were generated for patients in each stage. Results: Cancer distribution amongst 110 patients included lung cancer (n=50), GI cancers (n=42) and other cancers (n= 18). Cachexia stage distribution in patients was assessed (stage I= 45%, stage II =36% and stage III=18%). Patients with stage III cachexia had statistically significantly lower ECOG performance status (p=0.006), higher inflammatory state as measured by advanced lung cancer inflammation index (p<0.001), lower simplified nutritional appetite questionnaire (SNAQ score) (p=0.01), lower skeletal muscle index (p=0.03) and 30 seconds chair rise time (p<0.001). Median overall survival (OS) for stage I was 12.7 months, stage II 7.1 months and stage III 3.5 months (p=0.047). Conclusions: UTCCS system is a novel way of estimating the severity of cancer cachexia and correlates with inflammatory, dietary and functional parameters expected in patients with increasing severity of cancer cachexia.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 12046-12046
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

H

Harshit Khosla

2University of Texas Helath Science Center at Houston Medical, houston, United States

S

Syed Hasan Raza Jafri

University of Texas, Houston, TX

J

Julie Haewon Rowe

The University of Texas Health Science Center at Houston (UTHealth Houston) McGovern Medical School, Houston, TX

P

Putao Cen

The University of Texas Health Science Center at Houston (UTHealth Houston) McGovern Medical School, Houston, TX

J

Jessica Trevino Jones

UT San Antonio, San Antonio, TX

A

Anneliese Gonzalez

University of Texas Medical School at Houston, Houston, TX

N

Neha Maithel

University of Texas at Houston Health Science Center, McGovern Medical School, Houston, TX

R

Rabab Jafry

Aga Khan University Hospital, Karachi, Pakistan

B

Betty Arceneaux

UT Health, Houston, TX

S

Shahroz Aziz

The University of Texas Health Science Center at Houston, Houston, TX

M

Mina Hanna

The University of Texas Health Science Center at Houston, Houston, TX

A

Amirali Tahanan

The University of Texas Health Science Center at Houston, Houston, TX

Y

Yi-Ping Li

M

Mohammad Hossein Rahbar

The University of Texas Health Science Center at Houston, Houston, TX